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PreserFlo微型分流器用于开角型青光眼的五年随访

Five-year follow-up with the PreserFlo MicroShunt for open-angle glaucoma.

作者信息

Scheres Lotte M J, Kujovic-Aleksov Stefani, Winkens Bjorn, de Crom Ronald M P C, Webers Carroll A B, Beckers Henny J M

机构信息

University Eye Clinic Maastricht, Maastricht University Medical Center +, Maastricht, the Netherlands.

Department of Methodology and Statistics, Care and Public Health Research Institute (CAPHRI), Maastricht University, Maastricht, The Netherlands.

出版信息

Eye (Lond). 2025 Jun;39(8):1540-1546. doi: 10.1038/s41433-025-03707-3. Epub 2025 Feb 20.

Abstract

PURPOSE

To report on five-year results with the PreserFlo MicroShunt (MicroShunt) for the surgical treatment of open-angle glaucoma.

PATIENTS AND METHODS

Retrospective case series of consecutive patients who underwent a stand-alone MicroShunt implantation at the University Eye Clinic of Maastricht. If a patient underwent the procedure in both eyes, only the first eye was included in the analysis. MicroShunt implantation was augmented with 0.2 mg/ml mitomycin-C. The primary outcome was intraocular pressure (IOP) during follow-up. Furthermore, information on IOP-lowering medication use, success rates, reoperation rates, and postoperative complications was collected.

RESULTS

Sixty-six eyes were included for analyses. Diagnoses included primary open-angle glaucoma (88%) and pigmentary glaucoma (12%). The majority of patients had moderate or advanced glaucoma, based on the mean deviation of the visual field examination. Mean (95% - confidence interval) IOP dropped from 21.8 (20.8-22.8) at baseline to 13.2 (11.8-14.6) mmHg after 5 years (p < 0.001). Mean number of IOP-lowering medications was reduced from 2.5 (2.2-2.9) at baseline to 0.9 (0.5-1.2), 1.0 (0.7-1.4), and 1.1 (0.7-1.5) after three, four, and five years (all p < 0.001). Needling or surgical revision was performed in twelve eyes (18%). Nineteen eyes (29%) required further IOP-lowering surgery. Postoperative complications were usually mild and self-limiting and included early hypotony, shallow anterior chamber, and hyphaema.

CONCLUSIONS

After five years, the MicroShunt was found to be a safe procedure, leading to a sustained reduction in mean IOP and number of IOP-lowering medications. However, almost one third of the eyes required further IOP-lowering interventions.

摘要

目的

报告PreserFlo微型分流器(MicroShunt)用于开角型青光眼手术治疗的五年结果。

患者与方法

对在马斯特里赫特大学眼科诊所接受单独MicroShunt植入术的连续患者进行回顾性病例系列研究。如果患者双眼均接受了该手术,则仅将第一只眼纳入分析。MicroShunt植入术中使用0.2mg/ml的丝裂霉素C。主要结局是随访期间的眼压(IOP)。此外,收集了有关降低眼压药物使用情况、成功率、再次手术率和术后并发症的信息。

结果

66只眼纳入分析。诊断包括原发性开角型青光眼(88%)和色素性青光眼(12%)。根据视野检查的平均偏差,大多数患者患有中度或重度青光眼。平均(95%置信区间)眼压从基线时的21.8(20.8 - 22.8)mmHg降至5年后的13.2(11.8 - 14.6)mmHg(p < 0.001)。降低眼压药物的平均使用数量从基线时的2.5(2.2 - 2.9)降至三年、四年和五年后的0.9(0.5 - 1.2)、1.0(0.7 - 1.4)和1.1(0.7 - 1.5)(所有p < 0.001)。12只眼(18%)进行了针刺或手术修复。19只眼(29%)需要进一步的降低眼压手术。术后并发症通常较轻且为自限性,包括早期低眼压、前房浅和前房积血。

结论

五年后,发现MicroShunt手术安全,可使平均眼压和降低眼压药物的使用数量持续减少。然而,近三分之一的眼睛需要进一步的降低眼压干预。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b06f/12089333/9fc5f0b95d47/41433_2025_3707_Fig1_HTML.jpg

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